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Archives Francaises De Pediatrie
|
June 1, 1990
[Acute hepatic insufficiency disclosing congenital syphilis]
G Noseda, C Roy, P Phan, et al.
Neuroradiology
|
April 1, 1994
Acute bilateral striatal necrosis in an infant: CT and MRI
M T Sola Martínez, L Pierot, G Noseda, et al.
Annales De Genetique
|
January 1, 1982
[Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)]
M O Rethoré, J Lafourcade, J Couturier, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
December 9, 1982
[Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat]
M O Rethoré, J Lafourcade, J Couturier, et al.
Revue Neurologique
|
January 1, 1989
[Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)]
B Eymard, E Morel, O Dulac, et al.
Revue Neurologique
|
January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]
C Marsac, F Degoul, G Bonne, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 1, 1996
[Acute basal ganglia necrosis with favorable course during Mycoplasma encepahlitis]
G Noseda, J P Harpey, J P Brandel, et al.
Annales De Genetique
|
January 1, 1997
Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness
M Bahuau, D Vidaud, M Kujas, et al.
American Journal of Human Genetics
|
March 1, 1987
Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions
U Francke, J F Harper, B T Darras, et al.
Revue Neurologique
|
January 1, 1996
[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis]
M Fardeau, F M Tomé, A Helbling-Leclerc, et al.
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Search research articles
Search
Showing results (21-30 of 33) with videos related to
Sort By:
Page
of 4
Archives Francaises De Pediatrie
|
June 1, 1990
[Acute hepatic insufficiency disclosing congenital syphilis]
G Noseda, C Roy, P Phan, et al.
Neuroradiology
|
April 1, 1994
Acute bilateral striatal necrosis in an infant: CT and MRI
M T Sola Martínez, L Pierot, G Noseda, et al.
Annales De Genetique
|
January 1, 1982
[Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)]
M O Rethoré, J Lafourcade, J Couturier, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
December 9, 1982
[Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat]
M O Rethoré, J Lafourcade, J Couturier, et al.
Revue Neurologique
|
January 1, 1989
[Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)]
B Eymard, E Morel, O Dulac, et al.
Revue Neurologique
|
January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]
C Marsac, F Degoul, G Bonne, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 1, 1996
[Acute basal ganglia necrosis with favorable course during Mycoplasma encepahlitis]
G Noseda, J P Harpey, J P Brandel, et al.
Annales De Genetique
|
January 1, 1997
Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness
M Bahuau, D Vidaud, M Kujas, et al.
American Journal of Human Genetics
|
March 1, 1987
Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions
U Francke, J F Harper, B T Darras, et al.
Revue Neurologique
|
January 1, 1996
[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis]
M Fardeau, F M Tomé, A Helbling-Leclerc, et al.
Page
of 4